ArticleAmerican journal of human genetics2014
Utilizing population controls in rare-variant case-parent association tests.
Article in American journal of human genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed, 16 citations in OpenAlex.
- CLIN_SKAT: an R package to conduct association analysis using functionally relevant variants.BMC bioinformatics · 2022Article
- WISARD: workbench for integrated superfast association studies for related datasets.BMC medical genomics · 2018Article
- Adaptive combination of Bayes factors as a powerful method for the joint analysis of rare and common variants.Scientific reports · 2017Article
- Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data.European journal of human genetics : EJHG · 2017Article
- The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data.American journal of human genetics · 2017Article
- Increasing Generality and Power of Rare-Variant Tests by Utilizing Extended Pedigrees.American journal of human genetics · 2016Article
- Conditioning adaptive combination of P-values method to analyze case-parent trios with or without population controls.Scientific reports · 2016Article
- Beyond Rare-Variant Association Testing: Pinpointing Rare Causal Variants in Case-Control Sequencing Study.Scientific reports · 2016Article
- A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis.Bioinformatics (Oxford, England) · 2015Article
- A statistical approach for rare-variant association testing in affected sibships.American journal of human genetics · 2015Article
- Adaptive combination of P-values for family-based association testing with sequence data.PloS one · 2014Article
Corrections and comments
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Authors and funding
7 authors at 3 institutions in 1 country.
Funding
Abstract
There is great interest in detecting associations between human traits and rare genetic variation. To address the low power implicit in single-locus tests of rare genetic variants, many rare-variant association approaches attempt to accumulate information across a gene, often by taking linear combinations of single-locus contributions to a statistic. Using the right linear combination is key-an optimal test will up-weight true causal variants, down-weight neutral variants, and correctly assign the direction of effect for causal variants. Here, we propose a procedure that exploits data from population controls to estimate the linear combination to be used in an case-parent trio rare-variant association test. Specifically, we estimate the linear combination by comparing population control allele frequencies with allele frequencies in the parents of affected offspring. These estimates are then used to construct a rare-variant transmission disequilibrium test (rvTDT) in the case-parent data. Because the rvTDT is conditional on the parents' data, using parental data in estimating the linear combination does not affect the validity or asymptotic distribution of the rvTDT. By using simulation, we show that our new population-control-based rvTDT can dramatically improve power over rvTDTs that do not use population control information across a wide variety of genetic architectures. It also remains valid under population stratification. We apply the approach to a cohort of epileptic encephalopathy (EE) trios and find that dominant (or additive) inherited rare variants are unlikely to play a substantial role within EE genes previously identified through de novo mutation studies.
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